Vargas Natalie Rivera, Matos Moises, Kinaan Mustafa
Department of Internal Medicine, University of Central Florida College of Medicine, Orlando, Florida.
Internal Medicine Residency, University of Central Florida HCA Healthcare GME, Greater Orlando, Kissimmee, Florida.
AACE Clin Case Rep. 2024 Nov 2;11(1):58-61. doi: 10.1016/j.aace.2024.10.006. eCollection 2025 Jan-Feb.
BACKGROUND/OBJECTIVE: Papillary thyroid cancer (PTC) is considered the most common form of thyroid cancer. Papillary thyroid microcarcinomas (PTMCs) are defined as papillary carcinomas that are <1 cm and are often identified on surgical pathology but may be missed by ultrasound imaging.
Our case describes a 24-year-old woman who initially presented with a right lateral neck lump. This was thought to be a lipoma, and no workup was performed until it began to grow during pregnancy 3 to 4 years after initial presentation. The patient underwent excision with findings of a level 5B lymph node with pathology consistent with PTC, follicular variant. Neck ultrasound performed in an imaging center and in our clinic did not reveal thyroid nodules or abnormal appearing lymph nodes. Solid tumor profiling assay identified a neurotrophic tropomyosin receptor kinase (NTRK)-3 fusion: ETV6(4)-NTRK3(14) mutation.
PTMCs are identified with increased frequency due to improved ultrasound imaging and fine needle aspiration techniques. PTMCs are often associated with a benign course and are rarely metastatic. There has been growing interest in NTRK fusion mutations in PTC that has been associated with an increased risk of metastasis.
This case is unusual in that multiple cervical nodal metastases were present even without a sizable primary thyroid tumor. Although more studies are needed to elucidate the clinical and prognostic significance of NTRK fusion mutations in PTMC, their response to tropomyosin receptor kinase inhibitors may represent a future pathway for treatment.
背景/目的:甲状腺乳头状癌(PTC)被认为是甲状腺癌最常见的形式。甲状腺乳头状微小癌(PTMC)被定义为直径<1 cm的乳头状癌,常在手术病理中被发现,但超声成像可能会漏诊。
我们的病例描述了一名24岁女性,最初表现为右侧颈部肿块。该肿块被认为是脂肪瘤,在初次出现后3至4年怀孕期间开始生长之前未进行任何检查。患者接受了切除手术,发现5B级淋巴结,病理结果与滤泡变体PTC一致。在影像中心和我们诊所进行的颈部超声检查未发现甲状腺结节或异常的淋巴结。实体肿瘤分析检测发现神经营养性原肌球蛋白受体激酶(NTRK)-3融合:ETV6(4)-NTRK3(14)突变。
由于超声成像和细针穿刺技术的改进,PTMC的检出频率增加。PTMC通常病程良性,很少发生转移。人们对PTC中与转移风险增加相关的NTRK融合突变越来越感兴趣。
该病例不同寻常之处在于,即使没有明显的原发性甲状腺肿瘤,也存在多处颈部淋巴结转移。尽管需要更多研究来阐明PTMC中NTRK融合突变的临床和预后意义,但它们对原肌球蛋白受体激酶抑制剂的反应可能代表未来的治疗途径。